A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546579



Internal ID20919789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35841351..35844710hg38UCSC Ensembl
chr1:36306952..36310311hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251025
Samples
Known GenesAGO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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